Asymmetric synthesis of azetidin-2-ones by [2+2] cycloaddition using chiral imines derived from D-(+)-glucose

被引:33
作者
Arun, M
Joshi, SN
Puranik, VG
Bhawal, BM
Deshmukh, ARAS [1 ]
机构
[1] Natl Chem Lab, Div Organ Chem Synth, Pune 411008, Maharashtra, India
[2] Natl Chem Lab, Div Phys Chem, Pune 411008, Maharashtra, India
[3] Emcure Pharmaceut Ltd, Pune 411026, Maharashtra, India
关键词
asymmetric synthesis; ketenes; imines; Staudinger reaction;
D O I
10.1016/S0040-4020(03)00239-4
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Asymmetric synthesis of beta-lactams by the [2+2] cycloaddition of ketenes with chiral imines derived from D-(+)-glucose was carried out; predominantly cis-beta-lactams were formed with very high diastereoselectivity. The stereochemistry at C-3 and C-4 was established as 3S and 4R from the known absolute configuration of the sugar moiety. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2309 / 2316
页数:8
相关论文
共 35 条
[21]  
MANHAS MS, 1976, HETEROCYCLES, V5, P669
[22]  
MORIN RB, 1982, CHEM BIOL SSLACTUM A, V1
[23]  
Page M. I., 1992, CHEM SS LACTAMS
[24]   A β-lactam-based stereoselective access to β,γ-dihydroxy α-amino acid-derived peptides with either α,β-like or unlike configurations [J].
Palomo, C ;
Oiarbide, M ;
Landa, A ;
Esnal, A ;
Linden, A .
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (12) :4180-4186
[25]   ASYMMETRIC-SYNTHESIS OF MONOCYCLIC BETA-LACTAMS - APPLICATION OF IMINES DERIVED FROM CHIRAL N-PROTECTED ALPHA-AMINO ALDEHYDES IN THE STAUDINGER REACTION [J].
PALOMO, C ;
COSSIO, FP ;
CUEVAS, C .
TETRAHEDRON LETTERS, 1991, 32 (26) :3109-3110
[26]  
Palomo C., 1996, J ORG CHEM, V26, P61
[27]  
SCHIMIDT OT, 1963, METHODS CARBOHYDR CH, V2, P318
[28]  
Sheldrick G.M., 1997, Crystal Structure Refinement
[29]  
Southgate R., 1994, Contemp. Org. Synth., V1, p417 431, DOI [DOI 10.1039/CO9940100417, 10.1039/CO9940100417]
[30]   An efficient synthesis of cis-3-hydroxy-4-phenyl-beta-lactams: Precursor for taxol side chain [J].
Srirajan, V ;
Deshmukh, ARAS ;
Bhawal, BM .
TETRAHEDRON, 1996, 52 (15) :5585-5590